CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Fatal late-onset CAR T-cell-mediated encephalitis after axicabtagene-ciloleucel in a patient with large B-cell lymphoma.
Fatal late-onset CAR T-cell-mediated encephalitis after axicabtagene-ciloleucel in a patient with large B-cell lymphoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
以CD19为靶点的CAR-T 细胞治疗已成为多次复发/难治性大B细胞淋巴瘤(r/r LBCL)的标准治疗。该治疗的常见副作用是免疫效应细胞相关神经毒性综合征(ICANS)。在接受axicabtagene-ciloleucel(axi-cel)治疗的患者中,高达30%至40%可出现严重ICANS,通常发生在给药后最初4周内,且通常对类固醇反应良好。
我们描述了一例r/r LBCL患者在接受axi-cel输注9个月后出现进行性中枢神经毒性的病例,该患者此前曾接受过异基因造血细胞移植。尽管进行了广泛的全身和鞘内免疫抑制治疗,神经功能恶化仍不可逆转,并最终在5个月内致命。随着临床症状的出现,在脑脊液中发现了高CAR-T 细胞DNA拷贝数以及升高的白细胞介素-1(IL-1)和IL-6水平,尸检中观察到CAR-T 细胞脑浸润,提示CAR-T 细胞发挥了主要致病作用。这一意外的、毁灭性的迟发性神经毒性病例值得对CD19靶向CAR-T 细胞的神经系统脱靶效应进行更深入的研究,并强调需要对这一脆弱患者群体进行迟发性毒性的持续监测。
Treatment with CD19-directed (CAR) T cells has evolved as a standard of care for multiply relapsed or refractory large B-cell lymphoma (r/r LBCL). A common side effect of this treatment is the immune effector cell-associated neurotoxicity syndrome (ICANS). Severe ICANS can occur in up to 30% to 40% of patients treated with axicabtagene-ciloleucel (axi-cel), usually within the first 4 weeks after administration of the dose and usually responding well to steroids.
We describe a case of progressive central neurotoxicity occurring 9 months after axi-cel infusion in a patient with r/r LBCL who had undergone a prior allogeneic hematopoietic cell transplant. Despite extensive systemic and intrathecal immunosuppression, neurological deterioration was inexorable and eventually fatal within 5 months.
High CAR T-cell DNA copy numbers and elevated levels of interleukin-1 (IL-1) and IL-6 were found in the cerebral spinal fluid as clinical symptoms emerged, and CAR T-cell brain infiltration was observed on autopsy, suggesting that CAR T cells played a major pathogenetic role. This case of unexpected, devastating, late neurotoxicity warrants intensified investigation of neurological off-target effects of CD19-directed CAR T cells and highlights the need for continuous monitoring for late toxicities in this vulnerable patient population.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。